MicroScan B1017-411Recalls & reported problems
Beckman Coulter, Inc. · Neg Breakpoint Combo Panel Type 44 · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15099590657888), received between May 22, 2015 and May 22, 2015 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2015Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Patient Involvement
MAUDE report 4793485 ↗
Other Gram Negative Identification Panel devices
- VITEK® 2 GNBiomerieux , Inc. · Gram negative identification panel1 recall144 reports
- BD Phoenix™ NID 448007Becton, Dickinson And Company · GRAM NEGATIVE IDENTIFICATION PANEL138 reports
- BD BBL™ Crystal™ E/NF 245000Becton, Dickinson And Company · GRAM NEGATIVE IDENTIFICATION PANEL1 report
- MicroScan B1010-41ABeckman Coulter, Inc. · Gram Negative Identification Panel1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.